医学
哮喘
共病
内科学
皮质类固醇
儿科
药方
数据库
计算机科学
药理学
作者
Joan Sweeney,C. C. Patterson,Andrew Menzies‐Gow,Robert Niven,Adel Mansur,Christine Bucknall,Rekha Chaudhuri,David Price,Christopher E. Brightling,Liam G. Heaney
出处
期刊:Thorax
[BMJ]
日期:2016-01-27
卷期号:71 (4): 339-346
被引量:288
标识
DOI:10.1136/thoraxjnl-2015-207630
摘要
Objective
To determine the prevalence of systemic corticosteroid-induced morbidity in severe asthma. Design
Cross-sectional observational study. Setting
The primary care Optimum Patient Care Research Database and the British Thoracic Society Difficult Asthma Registry. Participants
Optimum Patient Care Research Database (7195 subjects in three age- and gender-matched groups)—severe asthma (Global Initiative for Asthma (GINA) treatment step 5 with four or more prescriptions/year of oral corticosteroids, n=808), mild/moderate asthma (GINA treatment step 2/3, n=3975) and non-asthma controls (n=2412). 770 subjects with severe asthma from the British Thoracic Society Difficult Asthma Registry (442 receiving daily oral corticosteroids to maintain disease control). Main outcome measures
Prevalence rates of morbidities associated with systemic steroid exposure were evaluated and reported separately for each group. Results
748/808 (93%) subjects with severe asthma had one or more condition linked to systemic corticosteroid exposure (mild/moderate asthma 3109/3975 (78%), non-asthma controls 1548/2412 (64%); p<0.001 for severe asthma versus non-asthma controls). Compared with mild/moderate asthma, morbidity rates for severe asthma were significantly higher for conditions associated with systemic steroid exposure (type II diabetes 10% vs 7%, OR=1.46 (95% CI 1.11 to 1.91), p<0.01; osteoporosis 16% vs 4%, OR=5.23, (95% CI 3.97 to 6.89), p<0.001; dyspeptic disorders (including gastric/duodenal ulceration) 65% vs 34%, OR=3.99, (95% CI 3.37 to 4.72), p<0.001; cataracts 9% vs 5%, OR=1.89, (95% CI 1.39 to 2.56), p<0.001). In the British Thoracic Society Difficult Asthma Registry similar prevalence rates were found, although, additionally, high rates of osteopenia (35%) and obstructive sleep apnoea (11%) were identified. Conclusions
Oral corticosteroid-related adverse events are common in severe asthma. New treatments which reduce exposure to oral corticosteroids may reduce the prevalence of these conditions and this should be considered in cost-effectiveness analyses of these new treatments.
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